Small Animal PET Scanner Research Articles

Study of two-layer tapered depth of interaction PET detector

Improving detection efficiency in small animal PET scanners without degrading spatial resolution is one of the main problems of these scanners. Commercial small animal PET scanners use different methods to achieve desirable levels of sensitivity and spatial resolution. GE Healthcare eXplore VISTA PET scanner uses double layer (LYSO-GSO) depth-of-interaction (DOI) capable cuboid detector modules. In this work, the design of GE Healthcare eXplore VISTA PET scanner is improved using tapered detector geometry instead of cuboid geometry. Using tapered detector geometry, the gaps between adjacent modules are filled and the sensitive volume has increased about 11.5%. The new designed PET scanner sensitivity and spatial resolution are studied for different crystal layer configurations (LYSO-GSO and GSO-LYSO with different thicknesses). As expected, average sensitivity over FOV is improved. Spatial resolution is slightly degraded but it is still uniform over FOV.

Development of a PET/EPRI combined imaging system for assessing tumor hypoxia

Precise quantitative delineation of tumor hypoxia is essential in radiation therapy treatment planningto improve the treatment efficacy by targeting hypoxic sub-volumes.We developed a combined imaging system of positron emission tomography (PET) and electron para-magnetic resonance imaging (EPRI) of molecular oxygento investigate the accuracy of PET imaging in assessing tumor hypoxia.The PET/EPRI combined imaging system aims to use EPRI to precisely measure the oxygen partial pressure in tissues.This will evaluate the validity of PET hypoxic tumor imaging by (near) simultaneously acquired EPRI as ground truth. The combined imaging system was constructed by integrating a small animal PET scanner (inner ring diameter 62 mm and axial field of view 25.6 mm)and an EPRI subsystem (field strength 25 mT and resonant frequency 700 MHz).The compatibility between the PET and EPRI subsystems were tested with both phantom and animal imaging.Hypoxic imaging on a tumor mouse model using 18F-fluoromisonidazole radio-tracerwas conducted with the developed PET/EPRI system.We report the development and initial imaging results obtained from the PET/EPRI combined imaging system.

Comparison of metabolic and functional parameters using cardiac 18F-FDG-PET in early to mid-adulthood male and female mice

BackgroundIn this descriptive study of male and female mice at different weeks of age, we use serial non-invasive cardiac 18F-FDG-PET scans to follow up on metabolic alterations, heart function parameters, and the ECG of both sexes in early to mid-adulthood.MethodsECG-gated 18F-FDG-PET scans were performed in mice on 10, 14, and 18 weeks of age, using a dedicated small-animal PET scanner. The percentage of the injected activity per gram (%IA/g) in the heart, left ventricular metabolic volume (LVMV), myocardial viability and left ventricular function parameters: end-diastolic (EDV), end-systolic (ESV), stroke volume (SV), and the ejection fraction (EF%) were estimated.ResultsCompared to their age-matched female counterpart, male mice showed a constant increase in LVMV and ventricular volume during the follow-up. In contrast, female mice remain stable after ten weeks of age. Furthermore, male mice showed lower heart rates, positive correlation with cardiac %IA/g, and negative correlation with LVMV.ConclusionIn this study of serial cardiac PET scans, we provide insight for basic murine research models, showing that mice gender and age show distinct cardiac metabolisms. These physiologic alterations need to be considered when planning in vivo injury models to avoid potential pitfalls.

Dynamic PET Image Reconstruction Incorporating Multiscale Superpixel Clusters

Dynamic positron emission tomography (PET) image reconstruction is challenging due to the low-count statistics of individual frames. This study proposes a novel reconstruction framework aiming to enhance the quantitative accuracy of individual dynamic frames via the introduction of priors based on multiscale superpixel clusters. The clusters are derived from pre-reconstruction composite images using superpixel clustering followed by fuzzy c-means (FCM) clustering. A multiscale aggregation is exploited during the superpixel clustering to generate multiscale superpixel clusters. Then, maximum a posteriori (MAP) PET reconstruction with different-scale clusters is separately applied to individual frame and fused to generate the final result. Using realistic simulated dynamic brain PET data, the quantitative performance of the proposed method is investigated and compared with the maximum-likelihood expectation-maximization (MLEM), Bowsher method, and kernelized expectation-maximization (the kernel method). The proposed method achieves substantial improvements in both visual and quantitative accuracy (in terms of the signal-to-noise ratio and contrast versus noise performances). The method is also tested with a 60 min 18F-FDG rat study performed with an Inveon small animal PET scanner. The proposed method is shown to outperform the other methods via improvements in visual and quantitative accuracy (in terms of noise versus the mean intensity of the region of interest).

Synthesis of [18F]F-γ-T-3, a Redox-Silent γ-Tocotrienol (γ-T-3) Vitamin E Analogue for Image-Based In Vivo Studies of Vitamin E Biodistribution and Dynamics.

Vitamin E, a natural antioxidant, is of interest to scientists, health care pundits and faddists; its nutritional and biomedical attributes may be validated, anecdotal or fantasy. Vitamin E is a mixture of tocopherols (TPs) and tocotrienols (T-3s), each class having four substitutional isomers (α-, β-, γ-, δ-). Vitamin E analogues attain only low concentrations in most tissues, necessitating exacting invasive techniques for analytical research. Quantitative positron emission tomography (PET) with an F-18-labeled molecular probe would expedite access to Vitamin E’s biodistributions and pharmacokinetics via non-invasive temporal imaging. (R)-6-(3-[18F]Fluoropropoxy)-2,7,8-trimethyl-2-(4,8,12-trimethyltrideca-3,7,11-trien-1-yl)-chromane ([18F]F-γ-T-3) was prepared for this purpose. [18F]F-γ-T-3 was synthesized from γ-T-3 in two steps: (i) 1,3-di-O-tosylpropane was introduced at C6-O to form TsO-γ-T-3, and (ii) reaction of this tosylate with [18F]fluoride in DMF/K222. Non-radioactive F-γ-T-3 was synthesized by reaction of γ-T-3 with 3-fluoropropyl methanesulfonate. [18F]F-γ-T-3 biodistribution in a murine tumor model was imaged using a small-animal PET scanner. F-γ-T-3 was prepared in 61% chemical yield. [18F]F-γ-T-3 was synthesized in acceptable radiochemical yield (RCY 12%) with high radiochemical purity (>99% RCP) in 45 min. Preliminary F-18 PET images in mice showed upper abdominal accumulation with evidence of renal clearance, only low concentrations in the thorax (lung/heart) and head, and rapid clearance from blood. [18F]F-γ-T-3 shows promise as an F-18 PET tracer for detailed in vivo studies of Vitamin E. The labeling procedure provides acceptable RCY, high RCP and pertinence to all eight Vitamin E analogues.

A GPU-accelerated fully 3D OSEM image reconstruction for a high-resolution small animal PET scanner using dual-ended readout detectors

In this work, a GPU-accelerated fully 3D ordered-subset expectation maximization (OSEM) image reconstruction with point spread function (PSF) modeling was developed for a small animal PET scanner with a long axial field of view (FOV). Dual-ended readout detectors that provided high depth of interaction (DOI) resolution were used for the small animal PET scanner to simultaneously achieve uniform high spatial resolution and high sensitivity. First, we developed a novel sinogram generation method, in which the dimension of the sinogram was determined first and then an event was assigned to a few neighboring sinogram elements by using weights that are inversely proportional to the distance from the measured line of response (LOR) to the LOR of the sinogram elements. System geometric symmetry, precomputation of LOR-driven ray-tracing and texture memory were applied to accelerate the GPU-based reconstruction. We developed a spatially variant PSF model where the PSF parameters were obtained by using point source images measured at 18 positions in the FOV and a spatial invariant PSF model where the PSF parameters were obtained by using only one image measured at the center FOV. The performance of the image reconstruction method was evaluated by using simulated phantom data as well as phantom and in-vivo mouse data acquired on the scanner. The results showed that the proposed reconstruction method provided better spatial resolution, a higher contrast recovery coefficient and lower noise than the OSEM reconstruction and was more than 1000 times faster than the CPU-based reconstruction. The spatially variant PSF model did not result in any spatial resolution improvement compared to the spatial invariant PSF model, and thus, the latter that is much easier to implement in image reconstruction and can be used in a small animal PET scanner using detectors with very high DOI resolution. A whole body 18F-FDG mouse image with high resolution and a high contrast to noise ratio was obtained by using the proposed reconstruction method.

Design and performance of SIAT aPET: a uniform high-resolution small animal PET scanner using dual-ended readout detectors

In this work, a small animal PET scanner named SIAT aPET was developed using dual-ended readout depth encoding detectors to simultaneously achieve high spatial resolution and high sensitivity. The scanner consists of four detector rings with 12 detector modules per ring; the ring diameter is 111 mm and the axial field of view (FOV) is 105.6 mm. The images are reconstructed using an ordered subset expectation maximization (OSEM) algorithm. The spatial resolution of the scanner was measured by using a 22Na point source at the center axial FOV with different radial offsets. The sensitivity of the scanner was measured at center axis of the scanner with different axial positions. The count rate performance of the system was evaluated by scanning mouse-sized and rat-sized phantoms. An ultra-micro hot-rods phantom and two mice injected with 18F-NaF and 18F-FDG were scanned on the scanner. An average depth of interaction (DOI) resolution of 1.96 mm, energy resolution of 19.1% and timing resolution of 1.20 ns were obtained for the detector. Average spatial resolutions of 0.82 mm and 1.16 mm were obtained up to a distance of 30 mm radially from the center of the FOV when reconstructing a point source in 1% and 10% warm backgrounds, respectively, using OSEM reconstruction with 16 subsets and 10 iterations. Sensitivities of 16.0% and 11.9% were achieved at center of the scanner for energy windows of 250–750 keV and 350–750 keV respectively. Peak noise equivalent count rates (NECRs) of 324 kcps and 144 kcps were obtained at an activity of 26.4 MBq for the mouse-sized and rat-sized phantoms. Rods of 1.0 mm diameter can be visually resolved from the image of the ultra-micro hot-rods phantom. The capability of the scanner was demonstrated by high quality in-vivo mouse images.

Design and measurement of Trans-PET basic detector module II using 6× 6 SiPM array for small-animal PET

Silicon photomultiplier (SiPM) coupled scintillation detectors, are considered as promising tools for basic design of imaging instrumentation for the next generation PET, PET/MRI, SPECT and autoradiography scanners. The precise technical knowledge is inadequate, and still some challenges need to be addressed in order to successfully implement the SiPM technology in high resolution PET systems. Firstly, the advantages of SiPM pixel array 1:1 coupled crystal detector were obvious, and has minimized the position resolution errors of charge sharing in multiplexing circuits. However, in the system level, too many electronic channels have perplexed with complications, such as complex, messy electronics or dedicated ASIC chips. Multiplexing circuits were usually used to lower the complexity and cost of electronics, which has resulted in gradual deterioration of the performances of the detectors. Secondly, the light guide has become a necessity in high-resolution preclinical PET detectors. For a complete SiPM detector block, the light yield of outermost two rows/columns crystals were blurred due to the edge effects. In order to avoid this edge deterioration effect, crystal array size was reduced than that of the SiPM array in many PET detectors. The PET system built by these detectors had big gaps between the detector modules, which has largely affected the quality of reconstructed images. In order to solve these key problems, the Trans-PET basic detection module (BDM) II was designed and implemented in this study. This module was a flexible, easy to upgrade, simple, box geometry, small animal PET scanner. A better balance could be achieved by this detector, while reducing the electronic channels, and could simultaneously enhance the position resolution and time performance. A specially customized semi-cutting light guide had been designed, which could be optically multiplexed and diffused to optimize the effect of edge deterioration, so that both the outermost and inner crystals could be clearly distinguished. Specifically, in this PET module, two type crystal arrays with different crystal size had been designed, 13× 13 crystal array with 1.89 mm width and 18× 18 crystal array with 1.2 mm width, based on the same 6× 6 SiPM array and frond-end electronics. The total area of 6× 6 SiPM was 25.0× 25.0 mm2, which was similar to Hamamatsu PSPMT R8900. The area of the SiPM array was slightly smaller than the size of the crystal array, in order to reduce the gap of the PET system built by this detector. The purpose of this study was to evaluate the performance of this detector module, including position profile quality, energy resolution, timing resolution in different operating environment. Based on this detector module, PET scanners can easily be designed with different shapes such as, quadrilaterals, hexagonals, octagonals, dodecagonals, twenty-four-sides, and other shapes.

TOF Benefits and Trade-offs on Image Contrast-to-Noise Ratio Performance for a Small Animal PET Scanner

Recently, time-of-flight (TOF) scanners have become a mainstream in positron emission tomography research particularly owing to their ability to improve the image contrast-to-noise ratio (CNR). As the scintillation photon transport directly affects the coincidence time resolution, decreasing crystal length can be considered to improve timing performance even at the cost of sensitivity loss. This would also improve the radial spatial resolution and reduce the cost of the scintillator material, particularly in clinical scanners. Hence, this article investigates the tradeoffs between TOF, crystal length, and scan time with the goal of using TOF to compensate for CNR degradation caused by decreasing the scintillator volume in a highly pixelated scanner. To do this, a TOF model of the LabPET II small animal scanner was developed. The contrast recovery coefficient (CRC) and CNR performance were investigated through a factorial design. This was followed by assessing when TOF gain may be advantageous in small animal imaging. Results show that decreasing crystal length by 2 mm improves CRC performance for such a scanner while CNR can be fully recovered by increasing scan time. It was also observed that the same CNR can be reached for a shorter acquisition time if faster TOF resolution is achieved. This article concludes with a summary of the trade offs to optimize the CNR.

Cross-Species Physiological Assessment of Brain Estrogen Receptor Expression Using 18F-FES and 18F-4FMFES PET Imaging.

A retrospective analysis was performed of preclinical and clinical data acquired during the evaluation of the estrogen receptor (ER) PET tracer 4-fluoro-11β-methoxy-16α-[18F]-fluoroestradiol (4FMFES) and its comparison with 16α-[18F]-fluoroestradiol (FES) in mice, rats, and humans with a focus on the brain uptake. Breast cancer tumor-bearing female BALB/c mice from a previous study and female Sprague-Dawley rats (control and ovariectomized) were imaged by 4FMFES or FES-PET imaging. Immediately after, low-dose CT was performed in the same bed position. Semi-quantitative analysis was conducted to extract %ID/g data. Small cohorts of mice and rats were imaged with 4FMFES in an ultra-high-resolution small animal PET scanner prototype (LabPET II). Rat brains were dissected and imaged separately with both PET and autoradiography. In parallel, 31 breast cancer patients were enrolled in a clinical phase II study to compare 4FMFES with FES for oncological assessment. Since the head was included in the field of view, brain uptake of discernable foci was measured and reported as SUVMax. Regardless of the species studied, 4FMFES and FES uptake were relatively uniform in most regions of the brain, except for bilateral foci at the base of the skull, at the midsection of the brain. Anatomical localization of the PET signal using CT image fusion indicates thatthe signal origins from the pituitary in all studied species. 4FMFES yielded lower pituitary uptake than FES in patients, but an inverse trend was observed in rodents. 4FMFES pituitary contrast was higher than FES in all assessed groups. High-resolution small animal imaging of the brain of rats and mice revealed a supplemental signal anterior to the pituitary, which is likely to be the medial preoptic area. Dissection data further confirmed those findings and revealed additional signals corresponding to the arcuate and ventromedial nuclei, along with the medial and cortical amygdala. 4FMFES allowed visualization of ER expression in the pituitary in humans and two different rodent species with better contrast than FES. Improvement in clinical spatial resolution might allow visualization and analysis of other ER-rich brain areas in humans. Further work is now possible to link 4FMFES pituitary uptake to cognitive functions.

Depth of Interaction Estimation in a Preclinical PET Scanner Equipped with Monolithic Crystals Coupled to SiPMs Using a Deep Neural Network

The scintillation light distribution produced by photodetectors in positron emission tomography (PET) provides the depth of interaction (DOI) information required for high-resolution imaging. The goal of positioning techniques is to reverse the photodetector signal’s pattern map to the coordinates of the incident photon energy position. By considering the DOI information, monolithic crystals offer good spatial, energy, and timing resolution along with high sensitivity. In this work, a supervised deep neural network was used for the approximation of DOI and to assess through Monte Carlo (MC) simulations the performance on a small-animal PET scanner consisting of ten 50 × 50 × 10 mm3 continuous Lutetium-Yttrium Oxyorthosilicate doped with Cerium (LYSO: Ce) crystals and 12 × 12 silicon photomultiplier (SiPM) arrays. The scintillation position was predicted by a multilayer perceptron neural network with 256 units and 4 layers whose inputs were the number of fired pixels on the SiPM plane and the total deposited energy. A GEANT4 MC code was used to generate training and test datasets by altering the photons’ incident position, energy, and direction, as well as readout of the photodetector output. The calculated spatial resolutions in the X-Y plane and along the Z-axis were 0.96 and 1.02 mm, respectively. Our results demonstrated that using a multilayer perceptron (MLP)-based positioning algorithm in the detector modules, constituting the PET scanner, enhances the spatial resolution by approximately 18% while the absolute sensitivity remains constant. The proposed algorithm proved its ability to predict the DOI for depth under 7 mm with an error below 8.7%.

Quality control of small animal PET scanner: The Brazilian Scenario

This work aims to evaluate the quality control program for small animal PET (positron emission tomography) scanners in Brazil. A questionnaire focused on type of small animal PET scanner and quality assurance program was prepared and sent to all Brazilian preclinical molecular imaging services that participated in the first Brazilian microPET/SPECT/CT users meeting held at the Federal University of Rio de Janeiro. The answers were compiled and descriptive statistic was applied. There are six preclinical molecular imaging services using PET scanner in Brazil. Five are in the southeastern region and one in the southern region. All services have a single PET device, but most of them have hybrids modalities with CT (computed tomography) and/or SPECT (single photon emission computed tomography). All services have knowledge of the NEMA NU 4-2008 publication specific to small animal PET equipments. However, most of them do not have a quality assurance program in place for their imaging systems. There are few preclinical PET devices installed in Brazil and most of them are located at southeastern region. Regardless the absence of quality assurance program in many of the services, there is a consensus on the importance of quality control program implementation.

Image quality evaluation of a small animal PET scanner

Performance testing of small animal PET scanners is very important to ensure the high performance required for this particular type of PET scanner. In this sense, National Electrical Manufactures Association (NEMA) published its NU 4/2008 standards, a consistent and standardized methodology for measuring scanner performance parameters for small animal PET imaging. Imaging capabilities of the scanner LabPET SOLO 4 were tested during two years according NEMA NU 4/2008 methodology. Results indicates that the equipment, despite a decade of use, presents performance appropriated and similar to performance of equipments reported in Literature.

Comments on the NEMA NU 4-2008 Standard on Performance Measurement of Small Animal Positron Emission Tomographs

The National Electrical Manufacturers Association’s (NEMA) NU 4-2008 standard specifies methodology for evaluating the performance of small-animal PET scanners. The standard’s goal is to enable comparison of different PET scanners over a wide range of technologies and geometries used. In this work, we discuss if the NEMA standard meets these goals and we point out potential flaws and improvements to the standard.For the evaluation of spatial resolution, the NEMA standard mandates the use of filtered backprojection reconstruction. This reconstruction method can introduce star-like artifacts for detectors with an anisotropic spatial resolution, usually caused by parallax error. These artifacts can then cause a strong dependence of the resulting spatial resolution on the size of the projection window in image space, whose size is not fully specified in the NEMA standard. If the PET ring has detectors which are perpendicular to a Cartesian axis, then the resolution along this axis will typically improve with larger projection windows.We show that the standard’s equations for the estimation of the random rate for PET systems with intrinsic radioactivity are circular and not satisfiable. However, a modified version can still be used to determine an approximation of the random rates under the assumption of negligible random rates for small activities and a constant scatter fraction. We compare the resulting estimated random rates to random rates obtained using a delayed coincidence window and two methods based on the singles rates. While these methods give similar estimates, the estimation method based on the NEMA equations overestimates the random rates.In the NEMA standard’s protocol for the evaluation of the sensitivity, the standard specifies to axially step a point source through the scanner and to take a different scan for each source position. Later, in the data analysis section, the standard does not specify clearly how the different scans have to be incorporated into the analysis, which can lead to unclear interpretations of publicized results.The standard’s definition of the recovery coefficients in the image quality phantom includes the maximum activity in a region of interest, which causes a positive correlation of noise and recovery coefficients. This leads to an unintended trade-off between desired uniformity, which is negatively correlated with variance (i.e., noise), and recovery.With this work, we want to start a discussion on possible improvements in a next version of the NEMA NU-4 standard.

Novel preclinical PET geometrical concept using a monolithic scintillator crystal offering concurrent enhancement in spatial resolution and detection sensitivity: a simulation study

We propose a small-animal PET scanner design combining two sets of monolithic crystals with two different thicknesses. The detectors with thinner crystals serve for high resolution imaging while the thicker crystals retain the detection efficiency. Two small-animal PET models based on 10 and 12 detector blocks made of monolithic LYSO crystals were implemented in the GEANT4 Monte Carlo toolkit. In each of these models, half of the detector blocks consisted of a crystal thickness of 10 mm whereas the second half had a crystal thickness of 2 mm. The scintillator crystals were coupled to SiPM arrays. For the first model, the detector blocks were arranged in a full-ring polygonal geometry in such a way that detector blocks with the same thickness were sitting opposite to each other. For the second model, detector blocks with different crystal thicknesses were facing each other. The performance of the proposed PET models was assessed using standard parameters, including spatial resolution, sensitivity and noise equivalent count rate. Comparison was made with conventional PET models with crystal thicknesses of 2 mm, 6 mm and 10 mm. PET models with a crystal thickness of 2 mm led to the highest spatial resolution (up to 0.6 mm FWHM) at the cost of poor absolute sensitivity (2.5%). On the other hand, PET models with a crystal thickness of 10 mm led to good detection efficiency (4.4%), yet with substantial degradation of spatial resolution (1.2 mm FWHM). The proposed PET models with thick and thin crystals exhibited an optimal trade-off between spatial resolution and sensitivity outperforming the PET model with fixed 6 mm crystal by achieving a spatial resolution of 0.7 mm and absolute sensitivity of 3.7%. The novel proposed PET design concept achieved an optimal trade-off between the sensitivity and spatial resolution by combining two sets of monolithic crystals.

Comparison of scandium-44\u2009g with other PET radionuclides in pre-clinical PET phantom imaging

PurposeThe decay characteristics of radionuclides in PET studies can impact image reconstruction. 44gSc has been the topic of recent research due to potential theranostic applications and is a promising radiometal for PET imaging. In this study, the reconstructed images from phantom measurements with scandium in a small-animal PET scanner are compared with 18F and two prominent radiometals: 64Cu and 68GaMethodsThree phantoms filled with 18F, 64C, 68Ga, and 44gSc were imaged in the Siemens Inveon PET scanner. The NEMA image quality phantom was used to determine the recovery coefficients (RCs), spill-over ratios (SORs), and noise (%SD) under typical pre-clinical imaging conditions. Image contrast was determined using a Derenzo phantom, while the coincidence characteristics were investigated using an NEC phantom. Three reconstruction algorithms were used, namely filtered back projection (FBP), ordered subset expectation maximization (OSEM), and maximum a-posteriori (MAP).ResultsImage quality parameters were measured for 18F, 64Cu, 68Ga, and 44gSc respectively; using FBP, the %SD are 5.65, 5.88, 7.28, and 7.70; the RCs for the 5-mm rod are 0.849, 1.01, 0.615, and 0.825; the SORs in water are 0.0473, 0.0595, 0.141, 0.0923; and the SORs in air are 0.0589, 0.0484, 0.0525, and 0.0509. The contrast measured in the 2.5-mm rods are 0.674, 0.637, 0.196, and 0.347. The NEC rate with 44gSc increased at a slower rate than 18F and 68Ga as a function of activity in the field of view.Conclusion44gSc demonstrates intermediate behavior relative to 18F and 68Ga with regard to RC and contrast measurements. It is a promising radionuclide for preclinical imaging.

Imaging Salt Uptake Dynamics in Plants Using PET

Soil salinity is a global environmental challenge for crop production. Understanding the uptake and transport properties of salt in plants is crucial to evaluate their potential for growth in high salinity soils and as a basis for engineering varieties with increased salt tolerance. Positron emission tomography (PET), traditionally used in medical and animal imaging applications for assessing and quantifying the dynamic bio-distribution of molecular species, has the potential to provide useful measurements of salt transport dynamics in an intact plant. Here we report on the feasibility of studying the dynamic transport of 22Na in millet using PET. Twenty-four green foxtail (Setaria viridis L. Beauv.) plants, 12 of each of two different accessions, were incubated in a growth solution containing 22Na+ ions and imaged at 5 time points over a 2-week period using a high-resolution small animal PET scanner. The reconstructed PET images showed clear evidence of sodium transport throughout the whole plant over time. Quantitative region-of-interest analysis of the PET data confirmed a strong correlation between total 22Na activity in the plants and time. Our results showed consistent salt transport dynamics within plants of the same variety and important differences between the accessions. These differences were corroborated by independent measurement of Na+ content and expression of the NHX transcript, a gene implicated in sodium transport. Our results demonstrate that PET can be used to quantitatively evaluate the transport of sodium in plants over time and, potentially, to discern differing salt-tolerance properties between plant varieties. In this paper, we also address the practical radiation safety aspects of working with 22Na in the context of plant imaging and describe a robust pipeline for handling and incubating plants. We conclude that PET is a promising and practical candidate technology to complement more traditional salt analysis methods and provide insights into systems-level salt transport mechanisms in intact plants.

Development of the Thin TOF-PET scanner based on fast monolithic silicon pixel sensors

The Thin-TOF PET (TT-PET) project aims at the construction of a small-animal PET scanner based on silicon monolithic pixel sensors with 30ps time resolution for 511keV photons, equivalent to 100ps time resolution for minimum ionizing particles. Iterative image reconstruction on Monte-Carlo simulation shows that the scanner can produce high signal-to-noise ratio images with good spatial resolution throughout the whole field of view. The demonstrator chip, comprising a 3 × 10 pixel matrix and a 50ps binning TDC, was tested at the CERN SPS beam test facility. The demonstrator shows an efficiency greater than 99.9% and a time resolution for minimum ionizing particles of approximately 110ps.

A monolithic ASIC demonstrator for the Thin Time-of-Flight PET scanner

Time-of-flight measurement is an important advancement in PET scanners to improve image reconstruction with a lower delivered radiation dose. This article describes the monolithic ASIC for the TT-PET project, a novel idea for a high-precision PET scanner for small animals. The chip uses a SiGe Bi-CMOS process for timing measurements, integrating a fully-depleted pixel matrix with a low-power BJT-based front-end per channel, integrated on the same 100 μm thick die. The target timing resolution of the scanner is 30 ps RMS for electrons from the conversion of 511 keV photons. The system will include 1.6 million channels across almost 2000 different chips. A full-featured demonstrator chip with a 3×10 matrix of 500×500 μm2 pixels was fabricated to validate each block. Its design and experimental results are presented here.

Image quality assessment using NEMA NU 4/2008 standards in small animal PET scanner

In Brazil, there are few microPET in use and a quality control protocols standardization are needed to harmonize their use in the research field. Thus, the purpose of this study is to characterize the image quality performance of the microPET scanner (LabPET 4, GE healthcare Technologies, Waukesha, WI) using the NEMA NU 4/ 2008 standards and specific phantom. The NEMA image-quality (IQ) phantom consists of 3 different regions to analyze distinct characteristics: image noise (%SD), expressed as percentage SD in a uniform region (%SD), recovery coefficient (RC) and Spill-over (SOR) in air and water. The IQ phantom was filled with 18F-FDG calibrated at the beginning of acquisition, placed in the center of the field-of-view (FOV) and measured with the typical whole body imaging protocol. The images were reconstructed with different reconstruction methods (FBP-2D; MLEM-3D and OSEM-3D); with and without high resolution (HR) when possible. The results were compared. The LabPET 4 system produces appropriate image and with performance according to the literature. The present study is an initial step to verify the NEMA NU 4/2008 use in the Brazilian scenario for further standardization.